DURAMER ADVANTIM POST. STAB. LSI TIBIAL INSERT 1890-3212

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1999-10-19 for DURAMER ADVANTIM POST. STAB. LSI TIBIAL INSERT 1890-3212 manufactured by Wright Medical Technology, Inc..

MAUDE Entry Details

Report Number1043534-1999-00098
MDR Report Key245793
Report Source06
Date Received1999-10-19
Date of Event1999-09-14
Date Mfgr Received1999-09-20
Device Manufacturer Date1995-12-01
Date Added to Maude1999-10-26
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional0
Initial Report to FDA0
Report to FDA0
Event Location0
Manufacturer ContactDEBBIE DAURER
Manufacturer Street5677 AIRLINE RD
Manufacturer CityARLINGTON TN 38002
Manufacturer CountryUS
Manufacturer Postal38002
Manufacturer Phone9018674601
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameDURAMER ADVANTIM POST. STAB. LSI TIBIAL INSERT
Generic NameKNEE COMPONENT
Product CodeKRP
Date Received1999-10-19
Model NumberNA
Catalog Number1890-3212
Lot Number125A032182
ID NumberNA
Device AvailabilityN
Device Eval'ed by MfgrN
Implant FlagY
Date Removed*
Device Sequence No1
Device Event Key238140
ManufacturerWRIGHT MEDICAL TECHNOLOGY, INC.
Manufacturer Address5677 AIRLINE RD ARLINGTON TN 38002 US
Baseline Brand NameDURAMER ADVANTIM POST STAB LSI TIBIAL INSERT
Baseline Generic NameKNEE COMPONENT
Baseline Catalog No1890-3212
Baseline Device FamilyK J 888.3560
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentY
Baseline TransitionalN
510k ExemptN


Patients

Patient NumberTreatmentOutcomeDate
10 1999-10-19

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